Syndrome XXYY - Unique The Rare Chromosome Disorder Support

The XXYY Syndrome also known as 48

We welcome new information on the impact of rare chromosome disorders on teeth. Please email Unique at info@rarechromo.org info@rarechromo.org.

Children with rare chromosome disorders are at risk for dental problems. In this group many children were affected and at least one child with abnormal enamel 

It is much less common than classical Klinefelter syndrome (47XXY). An estimated 1 in Rare Chromosome Disorder Support Group Charity Number 1110661.

diagnosis of Marfan syndrome based on his body habitus although he this condition by the Rare Chromosome Disorder Support Group

Rare Chromosome Disorder Support Group. PO Box 2189 Caterham

Rare Chromosome Disorder Support Group Charity Number 1110661 Unique publishes a separate guide: Looking after your child's teeth.

1p36 deletion syndrome affects 1 in 5000 live births and is thus classed as one of the more common deletion disorders (Unique

Apr 6 2022 48

Rare Chromosome Disorder Support Group Charity Number 1110661 It is much less common than classical Klinefelter syndrome (47XXY). An estimated one.